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HRID 338570作成日:2026年10月24日

Potassium Carbonate → Tert-butyl 3-(3-methylpyridin-4-yl)benzoate

https://huagongshe.com/ja/reaction/338570

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物4-Chloro-3-methylpyridineHCID 2757709—
反応物(3-((Tert-butoxy)carbonyl)phenyl)boronic acidHCID 2773299—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物Tert-butyl 3-(3-methylpyridin-4-yl)benzoateHCID 5789512171.4%

反応条件

温度80 °C

反応手順

4-Chloro-3-methylpyridine (2.00 g, 15.7 mmol), 3-(tert-butoxycarbonyl)phenylboronic acid (5.42 g, 24.4 mmol), a 2M aqueous solution of potassium carbonate (31.4 mL, 62.8 mmol), and palladium tetrakis(triphenylphosphine) (Pd(PPh3)4, 0.906 g, 0.784 mmol) were suspended in 1,2-dimethoxyethane (DME, 150 mL). The resulting mixture was stirred and heated to 80° C. for 60 hours. The crude reaction mixture was cooled to room temperature and then the layers were separated. The organic layer was evaporated to dryness and then purified on 120 g of silica gel utilizing a gradient of 0-70% ethyl acetate in hexanes to yield the pure product as a pale yellow oil (3.02 g, 11.2 mmol, 71.4%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08889875B2
出典データセットuspto-grants-2014_11
ORD IDord-ad087937869e45669e753b6ee4cfb5c9
出典メモuspto-grants-2014_11